FDA 510(k) Applications Submitted by NEOGUIDE SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K070622 03/06/2007 NEOGUIDE ENDOSCOPY SYSTEM NEOGUIDE SYSTEMS, INC.
K052930 10/19/2005 NAVIGATOR ENDOSCOPY SYSTEM NEOGUIDE SYSTEMS, INC.


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